lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: marlex pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
marlex pharmaceuticals, inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride 40 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
10135-736
Product ID
10135-736_4260de8c-7ec7-00d0-e063-6394a90aeebd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216250
Listing Expiration
2026-12-31
Marketing Start
2022-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
10135736
Hyphenated Format
10135-736
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
lidocaine hydrochloride (source: ndc)
Generic Name
lidocaine hydrochloride (source: ndc)
Application Number
ANDA216250 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (10135-736-51) / 50 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4260de8c-7ec7-00d0-e063-6394a90aeebd", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010878"], "spl_set_id": ["e1badbba-59af-e451-e053-2a95a90a49f8"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (10135-736-51) / 50 mL in 1 BOTTLE", "package_ndc": "10135-736-51", "marketing_start_date": "20220601"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "10135-736_4260de8c-7ec7-00d0-e063-6394a90aeebd", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "10135-736", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Marlex Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "40 mg/mL"}], "application_number": "ANDA216250", "marketing_category": "ANDA", "marketing_start_date": "20220601", "listing_expiration_date": "20261231"}